LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence

J Int Med Res. 2019 Jul;47(7):3299-3306. doi: 10.1177/0300060519847854. Epub 2019 Jun 20.

Abstract

Objectives: We investigated the role of long non-coding (lnc) RNA-NEF (neighboring enhancer of FoxA2), a characterized oncogene in cancer biology, in postmenopausal osteoporosis and its diagnostic and prognostic value in this disease.

Methods: Expression of lncRNA-NEF in plasma was detected by RNA extraction and real-time quantitative PCR. The diagnostic value of lncRNA-NEF and interleukin (IL)-6 for postmenopausal osteoporosis was evaluated by receiver operating characteristic curve analysis, with postmenopausal osteoporosis patients as true positive cases and healthy volunteers as true negative cases.

Results: We showed that plasma lncRNA-NEF was downregulated and plasma IL-6 was upregulated in postmenopausal osteoporosis patients compared with healthy controls. Altered plasma levels of lncRNA-NEF and IL-6 separated postmenopausal osteoporosis patients from healthy controls, and lncRNA-NEF and IL-6 were inversely and significantly correlated in osteoporosis patients. Patients were divided into high (n = 68) and low lncRNA-NEF (n = 73) groups according to Youden’s index. Patients with high lncRNA-NEF levels required a significantly shorter treatment course and had a lower post-treatment recurrence rate.

Conclusion: We showed that lncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence. The involvement of lncRNA-NEF in postmenopausal osteoporosis is likely related to IL-6.

Keywords: IL-6; Postmenopausal osteoporosis; lncRNA-NEF; long non-coding RNA; recurrence; treatment.

MeSH terms

  • Aged
  • Apoptosis
  • Calcitonin / analogs & derivatives*
  • Calcitonin / therapeutic use
  • Calcium-Regulating Hormones and Agents / therapeutic use
  • Case-Control Studies
  • Cell Proliferation
  • Cells, Cultured
  • Female
  • Follow-Up Studies
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Humans
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism*
  • Middle Aged
  • Osteoporosis, Postmenopausal / drug therapy
  • Osteoporosis, Postmenopausal / genetics*
  • Osteoporosis, Postmenopausal / pathology
  • Prognosis
  • RNA, Long Noncoding / genetics*
  • Recurrence

Substances

  • Calcium-Regulating Hormones and Agents
  • RNA, Long Noncoding
  • Calcitonin
  • elcatonin